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Synthesis and Characterization of Tunable, pH-Responsive Nanoparticle–Microgel Composites for Surface-Enhanced Raman Scattering Detection
[Image: see text] The synthesis of microgels with pH-tunable swelling leads to adjustable and pH-responsive substrates for surface-enhanced Raman scattering (SERS)-active nanoparticles (NPs). Sterically stabilized and cross-linked latexes were synthesized from random copolymers of styrene (S) and 2-...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645554/ https://www.ncbi.nlm.nih.gov/pubmed/31459181 http://dx.doi.org/10.1021/acsomega.8b01561 |
Sumario: | [Image: see text] The synthesis of microgels with pH-tunable swelling leads to adjustable and pH-responsive substrates for surface-enhanced Raman scattering (SERS)-active nanoparticles (NPs). Sterically stabilized and cross-linked latexes were synthesized from random copolymers of styrene (S) and 2-vinylpyridine (2VP). The pH-dependent latex-to-microgel transition and swellability were tuned based on their hydrophobic-to-hydrophilic content established by the S/2VP ratio. The electrostatic loading of polystyrene/poly(2-vinylpyridine) microgels [PS(x)P2VP(y) (M)] with anions such as tetrachloroaurate (AuCl(4)(–)) and borate-capped Ag NPs was quantified. The PS(x)P2VP(y) (M) can load ∼0.3 equiv of AuCl(4)(–) and the subsequent photoreduction results in Au NP-loaded PS(x)P2VP(y) (M) with NPs located throughout the structure. Loading PS(x)P2VP(y) (M) with borate-capped Ag NPs produces PS(x)P2VP(y) (M) with NPs located on the surface of the microgels, where the Ag content is set by S/2VP. The pH-responsive SERS activity is also reported for these Ag NP-loaded microgels. Analytical enhancement factors for dissolved crystal violet are high (i.e., 10(9) to 10(10)) and are set by S/2VP. The Ag NP-loaded microgels with ∼80 wt % 2VP exhibited the most stable pH dependent response. |
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